Pulmonary Research Group, University of Alberta, 559 Heritage Medical Research Centre, Edmonton, Alberta T6G 2S2, Canada.
J Inflamm (Lond). 2013 Jan 31;10(1):4. doi: 10.1186/1476-9255-10-4.
Eosinophils are often predominant inflammatory leukocytes infiltrating oral squamous carcinoma (OSC) sites. Prostaglandins are secreted by oral carcinomas and may be involved in eosinophil infiltration. The objective of this study was to determine the factors contributing to eosinophil migration and potential anti-neoplastic effects on OSC. Eosinophil degranulation was evaluated by measuring release of eosinophil peroxidase (EPO). Eosinophil chemotaxis towards OSC cells was assessed using artificial basement membrane. Eosinophil infiltration was prominent within the tissue surrounding the OSC tumor mass. We observed growth inhibition of the OSC cell line, SCC-9, during co-culture with human eosinophils, in vitro, which correlated with EPO activity that possesses growth inhibitory activity. The PGD2 synthase inhibitor, HQL-79, abrogated migration towards SCC-9. Our data suggest that OSC-derived PGD2 may play an important role via CRTH2 (the PGD2 receptor on eosinophils) in eosinophil recruitment and subsequent anti-tumor activity through the action of eosinophil cationic proteins.
嗜酸性粒细胞通常是浸润口腔鳞状细胞癌 (OSC) 部位的主要炎症性白细胞。前列腺素由口腔癌分泌,可能参与嗜酸性粒细胞浸润。本研究的目的是确定导致嗜酸性粒细胞迁移的因素,以及对 OSC 的潜在抗肿瘤作用。通过测量嗜酸性过氧化物酶 (EPO) 的释放来评估嗜酸性粒细胞脱颗粒。使用人工基底膜评估嗜酸性粒细胞向 OSC 细胞的趋化性。在 OSC 肿瘤块周围的组织中观察到嗜酸性粒细胞浸润明显。我们观察到,在体外与人嗜酸性粒细胞共培养时,OSC 细胞系 SCC-9 的生长受到抑制,这与具有生长抑制活性的 EPO 活性相关。PGD2 合酶抑制剂 HQL-79 阻断了向 SCC-9 的迁移。我们的数据表明,OSC 衍生的 PGD2 通过 CRTH2(嗜酸性粒细胞上的 PGD2 受体)在嗜酸性粒细胞募集中可能发挥重要作用,并且通过嗜酸性粒细胞阳离子蛋白的作用发挥随后的抗肿瘤活性。